Regulation and Control Flashcards

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1
Q

What is homeostasis?

A

A function of control systems in mammals to maintain a stable internal environment.

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2
Q

Why is constant temperature important?

A

Low temperatures slow metabolic reactions and high temperatures cause denaturation of proteins (enzymes)

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3
Q

Why is constant amount of water important?

A

Lack of water in tissue fluid causes water to be drawn out of cells (osmosis), slowing/stopping metabolic reactions. Too much water entering the cell can cause swelling/bursting.

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4
Q

Why is constant amount of glucose important?

A

Lack of glucose slows/stops respiration, depriving cell of energy source. Too much glucose may draw water out of cells by osmosis.

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5
Q

What is negative feedback?

A

A control loop used in control mechanisms in which a RECEPTOR picks up information about regulated parameter (INPUT), resulting in action by the EFFECTOR (OUTPUT).

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6
Q

What is excretion?

A

Elimination from the body of waste compounds produced during the metabolism of cells, including, for a human, carbon dioxide (excreted through the lungs) and urea (excreted through the kidneys in urine).

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7
Q

Why is removing nitrogenous waste products important?

A

Urea is produced by the liver from excess amino acids. There is more protein than needed, and the excess cannot be stored in the body as it is toxic.

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8
Q

Why is removing carbon dioxide important?

A

Carbon dioxide is not needed by the body, and produced by almost every cell. Transported from cells to lungs in bloodstream, diffuses into the alveoli and excreted when we breathe out.

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9
Q

What is a REFLEX ARC?

A

The pathway along which impulses are carried from a receptor to an effector without involving ‘conscious’ regions of the brain. e.g. in a spinal reflex arc, the impulse is carried from sensory neurone to intermediate neurones to motor neurones inside the spinal cord. In spinal cord, impulse will also be passed onto brain through other neurones. The effector responds to stimuli before any voluntary response. Useful for danger signals (eg hot object)

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10
Q

What are nerve impulses?

A

Very brief changes in the distribution of electrical charge across the plasma membrane, caused by movement of Na and K ions in/out of the axon.

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11
Q

What is the potential difference at RESTING POTENTIAL?

A

-65mV. The inside of the axon has a slightly negative electrical potential compared to the outside.

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12
Q

How is RESTING POTENTIAL maintained?

A

It is produced and maintained by the SODIUM-POTASSIUM PUMP in the plasma membrane of the axon. NA+ are picked up from cytoplasm inside axon by a CARRIER PROTEIN, and carried OUT. At the same time, K+ are brought into cytoplasm by external fluids. Both processes move ions against their concn gradient and require energy (hydrolysis of ATP). 3Na+ are removed for every 2K+ brought into cell and K+ diffuses out much faster than Na+ diffuses in, resulting in xs of +ve outside memb compared to inside.

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13
Q

What causes an ACTION POTENTIAL?

A

Electric current used to stimulate axon causes VOLTAGE-GATED CHANNELS (just the sodium channels) to open in the plasma memb to allow Na+ diffusion back into axon. The membrane is DEPOLARISED (less -ve tha before) and beings to build up positive charge.

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14
Q

What is the potential difference at ACTION POTENTIAL?

A

+40mV

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15
Q

How is the axon REPOLARISED? (2)

A

1) When potential difference reaches +40mV, SODIUM VOLTAGE GATED CHANNELS close and POTASSUM VOLTAGE GATED CHANNELS open. K+ diffuses out of the axon, removing +ve charge inside, beginning to return potential difference to normal. Membrane briefly becomes more -ve than normal at resting potential due to so many K+ ions diffusing out (REFRACTORY PERIOD). 2) POTASSIUM voltage gated channels close, and the SODIUM POTASSIUM PUMP begins restoring normal distribution of Na+ and K+ (resting potential).

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16
Q

How is an ACTION POTENTIAL transmitted along a neurone?

A

An action potential at any point on an axon’s plasma memb triggers production of action potential on either side. 2) causes a ‘local circuit’ to be set up between depolarised region and resting regions on either side. Na+ ions flow sideways inside axon, away from +vely charged region towards -ve regions on either side, depolarising these regions and generating an action potential.

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17
Q

How does the MYELIN SHEATH speed up the rate of conduction?

A

By insulating the axon membrane, so action potentials travel at up to 100m/s. Na and K ions cannot flow through myelin so action potentials only occur at the NODES OF RANVIER.

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18
Q

What is SALTATORY CONDUCTION?

A

When action potentials ‘jump’ from one node of Ranvier to the next due to myelinated areas, speeding transmission up by 50x.

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19
Q

Why is the REFRACTORY PERIOD important?

A

A ‘new’ action potential is only generated ahead of point of stimulation as region behind is in its REFRACTORY PERIOD ( Still be recovering from it’s action potential, and Na+ and K+ distribution will not yet be normal.)

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20
Q

How do RECEPTOR CELLS function?

A

They convert energy in one form (heat, light, sound) into energy in an electrical impulse in an neurone. They can be individual cells, or simply the ends of sensory neurones.

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21
Q

What is a PACINIAN CORPUSCLE?

A

It is found in the dermis of skin and contains the ending of a sensory neurone surrounded by several layers of connective tissue (CAPSULE, no myelin).

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22
Q

How does a PACINIAN CORPUSCLE function?

A

When pressure is applied, the CAPSULE is pressed out of shape and deforms nerve ending inside. This causes NA and K CHANNELS to open, allowing Na+ in and K+ out, depolarising membrane, causing increased positive charge in axon (RECEPTOR POTENTIAL). Above a pressure threshold, an ACTION POTENTIALS are initiated. (more pressure=higher frequency)

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23
Q

What is a TRANSMITTER SUBSTANCE?

A

Chemicals which pass action potential signals across synapses.

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24
Q

What is the PRESYNAPTIC NEURONE?

A

The neurone the transmitter substance is released from.

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25
Q

What is the POSTSYNAPTIC NEURONE?

A

The neuron in which an action potential is set up due to the release of the transmitter substance.

26
Q

What are CHOLINERGIC SYNAPSES?

A

Synapses which use ACETYLCHOLINE (ACh) as their transmitter substance, contained in vesicles in their cytoplasm.

27
Q

How are action potentials transmitted across synapses? (4)

A

1)When the action potential arrives in the membrane of the presynaptic neurone that is next to the synaptic cleft, it causes CALCIUM CHANNELS to open. 2) Influx of calcium ions causes vesicles of Ach to fuse with presynaptic membrane, and empty contents into synaptic cleft. Ach diffuses across the synaptic cleft. 3) Ach binds with RECEPTOR PROTEINS and opens SODIUM CHANNELS. Na+ ions rush in, depolarising membrane, starting off action potential. 4) Ach broken down by acetylcholinesterase (preventing continuous firing of action potential, and recycling Ach). Choline is taken back to presynaptic neurone and combine with acetyl co-enzyme A to form Ach again, which is transported into presynaptic vesicles.

28
Q

What are RECEPTOR PROTEINS?

A

Proteins in the plasma memb of the postsynaptic neurone. Part of it has a complementary shape to part of Ach molecule, so they can temporarily bind, changing shape of the protein opening Na channels.

29
Q

What is ACETYLCHOLINESTERASE?

A

An enzyme that splits Ach into acetate and choline (preventing continuous firing of action potential, and recycling Ach).

30
Q

What is the role of synapses? (3)

A

1) Ensures oneway transmission. 2) Increase possible range of actions in reponse to a stimulus.They allow intercollection of many nerve pathways (especially in the brain, for thinking). 3) Involved in memory and learning.

31
Q

What is an ENDOCRINE GLAND?

A

A gland containing specialised secretory cells that release a hormone directly into the blood stream at a distance from the hormone’s target organ.

32
Q

What are TARGET CELLS? (in context of hormones)

A

Cells on which a hormone has a particular effect.

33
Q

What are ISLETS OF LANGERHANS?

A

Cells scattered throughout pancreas, made up of α cells and β cells, responsible for the endocrine function of the pancreas.

34
Q

What does α cells secret?

A

Glucagon

35
Q

What does β cells secrete?

A

Insulin

36
Q

How does the pancreas respond to raised glucose levels? (3)

A

1) Raised levels detected by A and B cells when blood flows through pancreas. 2)B cells secrete INSULIN into blood plasma, which is carried to all part of body. A cells stop secreting glucagon. 3) Glucose levels drop.

37
Q

What is the effect of INSULIN? (3)

A

Insulin… 1) increases absorption of glucose from blood, 2) increases rate of respiration with glucose, 3) and increases rate at which glucose is converted to glycogen … among cells (especially liver and muscles).

38
Q

How does the pancreas respond to lowered glucose levels? (3)

A

1) Low levels detected by A and B cells when blood flows through pancreas. 2)A cells secrete GLUCAGON. B cells stop secreting insulin. 3) Glucose levels rise.

39
Q

What is the effect of GLUCAGON? (3)

A

Glucagon affects LIVER CELLS, and causes: 1) breakdown of glycogen to glucose 2) use of fatty acids instead of glucose as main fuel in respiration 3) production of gucose from other compounds (eg fats)

40
Q

Why are blood sugar levels never constant?

A

Inevitable time delay between change in blood glucose level and onset of corrective actions, resulting in oscillations.

41
Q

How do Beta cells detect high levels of glucose and release insulin in response? (5)

A

1)Normally, K+ CHANNELS are open in it’s plasma membrane, K+ diffuses out (outside more +ve), creating potential difference of -70mV. 2) When glucose levels are high around Beta cell, the glucose passes into the cell, and is quickly PHOSPHORYLATED by the enzyme GLUCOKINASE and METABOLISED to create ATP. 3)K+ CHANNELS are sensitive to amount of ATP in cell and respond by closing. Potential difference is reduced ( to -30mV). 4)New potential difference causes normally closed Ca2+ CHANNELS to open. Ca+ ions flood into cell from outside tissue fluid. 5)Ca2+ ions cause vesicles containing insulin to move to plasma membrane and fuse, emptying contents.

42
Q

What is ULTRAFILTRATION?

A

The filtering of small molecules (urea) out of the blood and into the renal capsule (Bowman’s capsule).

43
Q

Describe GLOMERULAR FILTRATION (3)

A

1) Fenestrations in capillary endothelium are large and let dissolved substances in blood plasma to move into the capsule (down the WP gradient) whie the basement membrane stops any large proteins from getting through (filters out erythrocytes etc.).
2) In gomerular capillaries, blood pressure is relatively high due to the wider diameter of afferent arteriole (to) compared to efferent arteriole (from), raising WATER POTENTIAL of blood plasma above WP of contents of Bowman’s capsule.
3) Even though concentration of solutes in blood is higher than solutes inside Bowman’s capsule (due to plasma proteins too big to get through), which lowers the WP of the blood, the effect of differences in pressure outweigh the effect of differences in solute concn.

44
Q

What is REABSORPTION?

A

Process of taking back any useful molecules from fluid in the nephron.

45
Q

What is the content of glomerular filtrate?

A

Identical to blood plasma, minus plasma proteins.

46
Q

What is the glomerular filtration rate?

A

125cm3/min

47
Q

Describe SELECTIVE REABSORPTION in the PROXIMAL CONVOLUTED TUBULE. (4)

A

1) Basal membranes (nearest blood) of cells lining the tubule ACTIVELY TRANSPORT Na+ out of the cell, into the blood.
2) Na+ from tubule filtrate PASSIVLEY diffuses back thourgh CARRIER PROTEINS in the membrane. These have several kinds, which transport different substances (eg glucose) as well as Na+ at the same time. The concn gradient for Na+ provides enough energy for glucose molecules to be tken up the cell, and into the blood. All glucose in glomerular filtrate is transported out of the tubule, ino the blood.
3) Water follows these substances out of the tubule through osmosis, down the concn gradient.
4) Urea (small) is also reabsorbed by its passive diffusion. Uric acid and creatinine are not.

48
Q

What is the function of the LOOP OF HENLE?

A

Loop of Henle allows water to be conserved in the body rather than it being lost in urine.

It creates a very high concentration of salts in the tissue fluid in the medulla. This allows alot of water to be reabsorbed from fluid in the COLLECTING DUCT as it flows through the medulla, creating concentrated urine.

The longer the loop, the greater the concn of urine that can be produced.

49
Q

Describe REABSORPTION in the LOOP OF HENLE

A

1) The upper parts of ASCENDING LIMB are IMPERMEABLE TO WATER.
2) Cells in walls of ascending limb actively transport Na+ and Cl- out of fluid of tube, into tissue fluid between cells filling space between the two limbs, producing a high concentration of Na+ and Cl- around DESCENDING LIMB. This is easy as concn in tissue fluid and loop are the same.
3) Walls of DESCENDING LIMB are PERMEABLE TO WATER, water is drawn out through osmosis into tissue fluid. Na+ and Cl- also diffuse into the tube.
4) The fluid is most concentrated at the bottom of the loop (H2O has diffused out and Na+/Cl- diffused in).
5) Fluid moves up ASCENDING LIMB, Na+/Cl- ions pass into tissue fluid (as fluid in limb is so concentrated).

Concentration of Na+ and Cl- throughout tube is never too different from the concn in adjacent tissue fluid, therefore not hard to remove.

50
Q

What is a COUNTER CURRENT MULTIPLIER?

A

The mechanism employed by the loop of Henle, two limbs running side by side, with fluid flowing down one and up the other.

51
Q

Describe SELECTIVE REABSORPTION in the COLLECTING DUCT.

A

1) The COLLECTING DUCT runs through the medulla, with a high solute concentration.
2) Water moves out of the duct by osmosis until the WP of urine (in duct) is the same as the WP in medulla tissue fluid. This is controlled by ADH.
3) It also pumps Na+ out and K+ in, like the second part of the DISTAL CONVOLUTED TUBULE.

52
Q

Describe SELECTIVE REABSORPTION in the DISTAL CONVOLUTED TUBULE.

A

1) First part of tubule behaves like ascending limb of loop of Henle.

2) Second part behaves like the collecting duct.
Na+ are actively pumped OUT from fluid in tubule to tissue fluid, where they pass into blood.

3) K+ are pumped INTO tubule.
4) This helps regulate the amount of these ions in blood.

53
Q

What is the path of the fluid going from the glomerulus? (6)

A

Glomerulus > Proximal convoluted tubule > Descending limb of loop of Henle > Ascending limb of loop of Henle > Dista convoluted tubule > Collecting Duct.

54
Q

What is OSMOREGULATION?

A

The regulation of water in the body fluids.

55
Q

What are the RECEPTORS and EFFECTORS in osmoregulation?

A

Receptor: hypothalamus (osmoreceptors)

Effector: Pituitary gland and walls of distal convoluted tubules/ collecting duct

56
Q

What does the nerve cells in the hypothalamus produce when they re stimulated by osmoreceptors?

A

Antidiuretic hormone, or ADH

57
Q

What is the effect of ADH?

A

It makes the plasma membranes of cells making up the wall of the collecting ducts more permeable to water than usual.

58
Q

How does ADH achieve its function? (5)

A

1) ADH is picked up by receptor on the plasma membrane, activating an enzyme within the cell.
2) Activation of enzyme causes vesicles in the cell (with AQUAPORINS - water-permeable channels in its membranes) to fuse with the plasma membrane of the cell, adding AQUAPORINS to it.
3) Water is free to move out of tubule, through cells lining the collecting duct, and into the tissue fluid, because this region of the kdiney contains a high concentration of salts.
4) When blood water content rises, osmoreceptors are no longer stimulated and stop stimulating nerve cells, ADH secretion slows down.
5) AQUAPORINS moved from plasma membrane of collecting duct cells and return to cytoplasm, and urine becomes more dilute. Not an immediate process

59
Q

How does NICOTINE affect synapse function?

A

part of the nicotine molecule is similar in shape to Ach, and fit into the Ach receptors on postsynaptic membranes, and produces similar effects to Ach.

However nicotine is not rapidly broken down by enzymes, and remaind in receptors for longer than Ach, large doses can be fatal.

60
Q

How does BOTULINUM TOXIN affect synapse function?

A
  • Produced by anaerobic bacteria in canned food.
  • Prevents release of Ach (acts on presynaptic membrane).
  • Injections of tiny amounts can help muscles relax (eq eye muscles relax, and eyes can be opened)
61
Q

What is the effect of ORGANOPHOSPHOROUS INSECTICIDES on synaptic function?

A

-Inhibits the actions of acetycholinesterase, allowing Ach to cause continuous production of action potential in the postsynaptic membrane. Nerve gases also act in this way.